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Steroid injection in knee now in more pain
A week last Thursday I had a steroid injection in my knee, it seemed to work but after a few days the pain is now much worse but not hot, especially when laying down and other knee hurting. Really worried as my daughters wedding is in 3 weeks next week. I’ve never had this problem before with an injection
A week last Thursday I had a steroid injection in my knee, it seemed to work but after a few days the pain is now much worse but not hot, especially when laying down and other knee hurting. Really worried as my daughters wedding is in 3 weeks next week. I’ve never had this problem before with an injection
Maggie153
in
Arthritis Action
6 years ago
Steroids!!!
Had a steroid injection and a course of prednisone , had a bad infection and had to come off all my meds mtx bio, but I've had this horrible eye twitch for last day or two driving me mad any one else had this prob thanx ????
Had a steroid injection and a course of prednisone , had a bad infection and had to come off all my meds mtx bio, but I've had this horrible eye twitch for last day or two driving me mad any one else had this prob thanx ????
Nsmith13
in
NRAS
6 years ago
Chapel Allerton
Hi guys and gals Sorry it’s late but had my appointment at rheumatology clinic today the consultant was lovely explained everything I’m going on a new injection as humira isn’t working also gonna have steroid injections in right hand I am dreading 😟 it I must say but if it helps all well and good nite
Hi guys and gals Sorry it’s late but had my appointment at rheumatology clinic today the consultant was lovely explained everything I’m going on a new injection as humira isn’t working also gonna have steroid injections in right hand I am dreading 😟 it I must say but if it helps all well and good nite
Deejojo
in
NRAS
6 years ago
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Biologics and sun sensitivity/allergies
Hi I am looking for some ideas. I have RA and have been on Cimzia since September. Also had general steroid injection about 3 weeks ago. In the last couple of weeks I have started to get itchy red patches on my hands and now the skin around my eyes is dry, and itchy with some areas of swelling of the
Hi I am looking for some ideas. I have RA and have been on Cimzia since September. Also had general steroid injection about 3 weeks ago. In the last couple of weeks I have started to get itchy red patches on my hands and now the skin around my eyes is dry, and itchy with some areas of swelling of the
Mouseling
in
NRAS
6 years ago
Follow up to lumbar steroid injections, Day 2
I feel great! My back feels so much better!! I had to discontinue my RA meds for about 4-5 days prior to the procedure and I'm wondering if being off them is what is making me feel better or if it's the overall feeling of the steroids throughout my body that is making me feel better overall. The good
I feel great! My back feels so much better!! I had to discontinue my RA meds for about 4-5 days prior to the procedure and I'm wondering if being off them is what is making me feel better or if it's the overall feeling of the steroids throughout my body that is making me feel better overall. The good
Radiogirl
in
NRAS
6 years ago
Not sure what to do next
This is my first post even though I have been a member for some time and have studied people's posts who have similar conditions to my own. I am 57 years and female. I was first diagnosed with osteoarthritis in my left knee in 1992 and until the last 18 months has slowly got worse. Since this time I
This is my first post even though I have been a member for some time and have studied people's posts who have similar conditions to my own. I am 57 years and female. I was first diagnosed with osteoarthritis in my left knee in 1992 and until the last 18 months has slowly got worse. Since this time I
G-String
in
Arthritis Action
6 years ago
Steroid injection v pain killers
I would appreciate some advice or opinions on treatment I've been offered. I'm 3 years into PMR and down to 3.5mg prednisolone. I've recently been diagnosed with osteoarthritis of the hips (I'm 58) I've been taking at least 4 paracetamol and 4 ibuprofen every day, which is enabling me to be fairly comfortable
I would appreciate some advice or opinions on treatment I've been offered. I'm 3 years into PMR and down to 3.5mg prednisolone. I've recently been diagnosed with osteoarthritis of the hips (I'm 58) I've been taking at least 4 paracetamol and 4 ibuprofen every day, which is enabling me to be fairly comfortable
margiebell4
in
PMRGCAuk
6 years ago
Short syacthen test and hip steroid injections?
Hi I was sent to see NHS endo in Oxford....She told me that I seemed very well informed on Hashimoto's and use of T3 (thank you all administrators on here)! She did say that she does not recommend T3 only, but would give it if neccessary...I had given up getting correct treatment ages ago, so am self
Hi I was sent to see NHS endo in Oxford....She told me that I seemed very well informed on Hashimoto's and use of T3 (thank you all administrators on here)! She did say that she does not recommend T3 only, but would give it if neccessary...I had given up getting correct treatment ages ago, so am self
PiggySue
in
Thyroid UK
6 years ago
Will UK Residence Help Me?
Hello all, In January of this year I had my entire life ruined overnight when I suddenly developed severe pain and urinary urgency which wasn't relieved with urinating. My symptoms were present 24/7 and didn't improve for many months. Constant pain and severe sleep deprivation left me feeling suicidal
Hello all, In January of this year I had my entire life ruined overnight when I suddenly developed severe pain and urinary urgency which wasn't relieved with urinating. My symptoms were present 24/7 and didn't improve for many months. Constant pain and severe sleep deprivation left me feeling suicidal
Hidden
in
Pelvic Pain Support Network
6 years ago
New, confused and hoping to pick your brains!
Hi everyone, I've been reading through various forums hoping to find an answer to my symptoms (aren't we all!) so given how kind and informed you all seem to be (from hard-won experience dealing with medics I'm guessing) I'm hoping you can offer me some guidance. I've had many, many tests, but I'm
Hi everyone, I've been reading through various forums hoping to find an answer to my symptoms (aren't we all!) so given how kind and informed you all seem to be (from hard-won experience dealing with medics I'm guessing) I'm hoping you can offer me some guidance. I've had many, many tests, but I'm
Cghkent
in
Thyroid UK
6 years ago
New, confused and hoping to pick your brains!
Hi everyone, I've been reading through various forums hoping to find an answer to my symptoms (aren't we all!) so given how kind and informed you all seem to be (from hard-won experience dealing with medics I'm guessing) I'm hoping you can offer me some guidance. I've had many, many tests, but I'm hoping
Hi everyone, I've been reading through various forums hoping to find an answer to my symptoms (aren't we all!) so given how kind and informed you all seem to be (from hard-won experience dealing with medics I'm guessing) I'm hoping you can offer me some guidance. I've had many, many tests, but I'm hoping
Cghkent
in
Pernicious Anaemia Society
6 years ago
Grief stricken and big flare !
I am full flare at the moment (housebound), I was diagnosed with RA in 2011 at Northampton Rheumatology Clinic, but moved to South Wales in 2016 and now attending RA clinic in Bridgend. My problem is my medication isn't covering my condition, I am on 20mg Methotrexate injection once a week with no other
I am full flare at the moment (housebound), I was diagnosed with RA in 2011 at Northampton Rheumatology Clinic, but moved to South Wales in 2016 and now attending RA clinic in Bridgend. My problem is my medication isn't covering my condition, I am on 20mg Methotrexate injection once a week with no other
petalnumber2
in
NRAS
6 years ago
Side effects 🤔
Hello everyone, I hope you are all as well as can be. I apologise in advance for the similar topic post to one I made two months ago, however after a delay in getting started (thanks to some confusion on my GP's part) on Azathioprine, I finally started taking it on Sunday night (I take it with my nightly
Hello everyone, I hope you are all as well as can be. I apologise in advance for the similar topic post to one I made two months ago, however after a delay in getting started (thanks to some confusion on my GP's part) on Azathioprine, I finally started taking it on Sunday night (I take it with my nightly
_jenc_
in
LUPUS UK
6 years ago
Hello...I'm a newbie here. Seeking Tinnitus help.
Hello all. I found your site after doing a search for Tinnitus on the NRAS page for Rheumatoid Arthritis/Rheumatoid Disease. I have had Tinnitus since December 2017/January 2018. I am seeing an ENT, but have only had one appointment so far. I am scheduled for a hearing test at my next appointment.
Hello all. I found your site after doing a search for Tinnitus on the NRAS page for Rheumatoid Arthritis/Rheumatoid Disease. I have had Tinnitus since December 2017/January 2018. I am seeing an ENT, but have only had one appointment so far. I am scheduled for a hearing test at my next appointment.
Radiogirl
in
British Tinnitus Association
6 years ago
Specialist nurse
Well folks I found out something interesting today, I phoned my GP to see if I could get a steroid injection today as I'm really struggling with pain and burning joints at the moment, he said he would rather hold off at the moment until I have an ultrasound which I'm waiting for as I have DVT which I've
Well folks I found out something interesting today, I phoned my GP to see if I could get a steroid injection today as I'm really struggling with pain and burning joints at the moment, he said he would rather hold off at the moment until I have an ultrasound which I'm waiting for as I have DVT which I've
popsmith1874
in
NRAS
6 years ago
New to Lupus and need advise
Hi All, I am 32 and have been recently been diagnosed with Lupus. I am still in denial about this and haven't fully accepted it and keep holding out that the doctors have got it wrong. I guess I have known for a long while that something was not quite right but chose to ignore the symptoms and carry
Hi All, I am 32 and have been recently been diagnosed with Lupus. I am still in denial about this and haven't fully accepted it and keep holding out that the doctors have got it wrong. I guess I have known for a long while that something was not quite right but chose to ignore the symptoms and carry
Jacpat
in
LUPUS UK
6 years ago
Injections
I have 3 disc prolapses ,all the sacral joints deterioration , nerve compression & kyphosis spasms I suspect due to underlying spina bifida, neurogenic bladder & retention.I only found this our after severe bouts of spasticity relieved with antibiotic /uti medication .At 71yrs I also have heart failure
I have 3 disc prolapses ,all the sacral joints deterioration , nerve compression & kyphosis spasms I suspect due to underlying spina bifida, neurogenic bladder & retention.I only found this our after severe bouts of spasticity relieved with antibiotic /uti medication .At 71yrs I also have heart failure
skybluepink
in
Neuro Support
6 years ago
Macrodactyly and Chronic Pain
Hi Guys, I'm new here... I have Macrodactyly on my left hand. Since 2010 I have been struggling with chronic pain. I use to get pain before, but it was only when the weather was changing/cold, if I overused my hand or if I clumsily slept on it. I have a lot of scar tissue and nerve damage which is the
Hi Guys, I'm new here... I have Macrodactyly on my left hand. Since 2010 I have been struggling with chronic pain. I use to get pain before, but it was only when the weather was changing/cold, if I overused my hand or if I clumsily slept on it. I have a lot of scar tissue and nerve damage which is the
KIM92
in
Pain Concern
6 years ago
Therapy Options.
One of the constant questions we hear in this chat room is about Therapies, what effect this therapy has or what effects that there has and the Pros vs the cons of each therapy. Now to keep this free coming at 12 page post I would hope that everyone could try to keep their answers direct and to the point
One of the constant questions we hear in this chat room is about Therapies, what effect this therapy has or what effects that there has and the Pros vs the cons of each therapy. Now to keep this free coming at 12 page post I would hope that everyone could try to keep their answers direct and to the point
Fancy1959
CommunityAmbassador
in
My MSAA Community
6 years ago
Hydroxychloroquine for fatigue?
Hi folks, I am not diagnosed yet but I have some blood markers (positive ENA and anti-RO) for Lupus or Sjogren's. (more symptoms of Lupus but playing the waiting game) When I last saw the rheumatologist he gave me three options, do nothing, try a steroid injection, try hydroxychloroquine. He gave me
Hi folks, I am not diagnosed yet but I have some blood markers (positive ENA and anti-RO) for Lupus or Sjogren's. (more symptoms of Lupus but playing the waiting game) When I last saw the rheumatologist he gave me three options, do nothing, try a steroid injection, try hydroxychloroquine. He gave me
AmyG6500
in
LUPUS UK
6 years ago
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